479969
4-氨基-5-嘧啶甲腈
96%
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关于此项目
经验公式（希尔记法）:
C5H4N4
化学文摘社编号:
分子量:
120.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
Form:
solid
InChI
1S/C5H4N4/c6-1-4-2-8-3-9-5(4)7/h2-3H,(H2,7,8,9)
SMILES string
Nc1ncncc1C#N
InChI key
JAIYUIOGVNRXEW-UHFFFAOYSA-N
assay
96%
form
solid
mp
251-255 °C (lit.)
functional group
nitrile
Application
4-Amino-5-pyrimidinecarbonitrile may be used as a monodentate ligand to prepare metal complexes of Co(II), Ni(II), Cu(II) and Pd(II) ions. It may be used as a reactant to prepare 1H-pyrimido[4,5-d]pyrimidine-2,4-dione.
General description
4-Amino-5-pyrimidinecarbonitrile (APC) is a pyrimidine derivative that has been synthesized via three-component reaction between benzaldehyde, benzamidine hydrochloride and malononitrile. The infrared, 1H NMR, 13C NMR and mass spectra of APC have been recorded.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
Synthesis of quinazoline-2,4(1H,3H)-diones from carbon dioxide and 2-aminobenzonitriles using [Bmim]OH as a homogeneous recyclable catalyst.
Patil YP, et al.
Catalysis Today, 148(3), 355-360 (2009)
Three-component process for the synthesis of 4-amino-5-pyrimidinecarbonitriles under thermal aqueous conditions or microwave irradiation.
Sheibani H, et al.
ARKIVOC (Gainesville, FL, United States), 2, 115-123 (2008)
Synthesis, antimicrobial activity, structural and spectral characterization and DFT calculations of Co (II), Ni (II), Cu (II) and Pd (II) complexes of 4-amino-5-pyrimidinecarbonitrile.
Mohamed TA, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 135, 417-427 (2015)
Infrared and NMR spectra, tautomerism, vibrational assignment, normal coordinate analysis, and quantum mechanical calculations of 4-amino-5-pyrimidinecarbonitrile.
Afifi MS, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 111, 277-289 (2013)
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